Urano T, Furukawa K, Shiku H
Department of Oncology, Nagasaki University School of Medicine, Japan.
Oncogene. 1993 May;8(5):1371-6.
We determined whether proteins encoded by the nm23/nucleoside diphosphate (NDP) kinase gene, a potential metastasis-suppressor gene, are expressed on the cell surface. Monoclonal antibodies (mAb) specific for nm23-H1 or H2 proteins were prepared using the corresponding fusion proteins with glutathione S-transferase (GST) as immunogens. mAb H1-229 was specifically reactive with nm23-H1 protein, whereas mAb H2-439 was specific for nm23-H2 protein in immunoprecipitation and immunoblotting. mAb H1-229 was reactive with most human hematopoietic and some non-hematopoietic cell lines in flow cytometry. On the other hand, mAb H2-439 was reactive with only a limited number of cell lines. Based upon the surface expression of nm23/NDP kinase, cells were classified as nm23-H1+H2-, nm23-H1+H2+ or nm23-H1-H2-. No cell lines with nm23-H1-H2+ were found among those examined. The specificity of flow cytometry analysis was confirmed in the murine myeloma line NS-1 transfected with either the nm23-H1 or H2 genes. Both mAbs were reactive only to NS-1 transfected with the corresponding nm23 genes. Immunoprecipitation and SDS-PAGE analysis identified 20.5- and 18-kDa proteins with mAb H1-229 or H2-439, respectively, in cellular extracts of 125I-surface labeled NS-1 transfected with the corresponding genes. The presence of nm23/NDP kinase on the cell surface indicates an extracellular role for these proteins in addition to their reported intracellular functions.
我们确定了一种潜在的转移抑制基因——nm23/核苷二磷酸(NDP)激酶基因所编码的蛋白质是否在细胞表面表达。以与谷胱甘肽S-转移酶(GST)的相应融合蛋白作为免疫原,制备了对nm23-H1或H2蛋白具有特异性的单克隆抗体(mAb)。在免疫沉淀和免疫印迹中,mAb H1-229与nm23-H1蛋白具有特异性反应,而mAb H2-439对nm23-H2蛋白具有特异性。在流式细胞术中,mAb H1-229与大多数人类造血细胞系和一些非造血细胞系有反应。另一方面,mAb H2-439仅与有限数量的细胞系有反应。根据nm23/NDP激酶的表面表达情况,细胞被分类为nm23-H1+H2-、nm23-H1+H2+或nm23-H1-H2-。在所检测的细胞系中未发现nm23-H1-H2+的细胞系。在转染了nm23-H1或H2基因的小鼠骨髓瘤细胞系NS-1中证实了流式细胞术分析的特异性。两种单克隆抗体仅对转染了相应nm23基因的NS-1有反应。免疫沉淀和SDS-PAGE分析分别在转染了相应基因的125I表面标记的NS-1的细胞提取物中,用mAb H1-229或H2-439鉴定出了20.5 kDa和18 kDa的蛋白质。nm23/NDP激酶在细胞表面的存在表明这些蛋白质除了其已报道的细胞内功能外,在细胞外也发挥作用。